International safety notice
Lot Recall for ProTack fixation device, Covidien
Germany / BfArM · DEU · Aug 6, 2010
Key facts
| Title | Lot Recall for ProTack fixation device, Covidien |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ProTack fixation device, Covidien |
| Manufacturer | Lot Recall for ProTack fixation device, Covidien |
| Models | POB0753, P9H1081, P9M0112, 174006, POA0021, POA0723 |
| Date | Aug 6, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1